CH653005A5 - Oxydehydrogenation catalyst, and process for the catalytic conversion of isobutyric acid or functional derivatives thereof into corresponding alpha, beta-unsaturated compounds - Google Patents
Oxydehydrogenation catalyst, and process for the catalytic conversion of isobutyric acid or functional derivatives thereof into corresponding alpha, beta-unsaturated compounds Download PDFInfo
- Publication number
- CH653005A5 CH653005A5 CH6706/81A CH670681A CH653005A5 CH 653005 A5 CH653005 A5 CH 653005A5 CH 6706/81 A CH6706/81 A CH 6706/81A CH 670681 A CH670681 A CH 670681A CH 653005 A5 CH653005 A5 CH 653005A5
- Authority
- CH
- Switzerland
- Prior art keywords
- catalyst
- isobutyric acid
- oxydehydrogenation
- reaction
- substrate
- Prior art date
Links
- 239000003054 catalyst Substances 0.000 title claims abstract description 49
- 238000006243 chemical reaction Methods 0.000 title claims abstract description 31
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 title claims abstract description 31
- 238000000034 method Methods 0.000 title claims description 44
- 230000003197 catalytic effect Effects 0.000 title claims description 5
- 150000001875 compounds Chemical class 0.000 title claims description 3
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229910052709 silver Inorganic materials 0.000 claims abstract description 12
- 239000004332 silver Substances 0.000 claims abstract description 12
- 239000010941 cobalt Substances 0.000 claims abstract description 10
- 229910017052 cobalt Inorganic materials 0.000 claims abstract description 10
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229910052746 lanthanum Inorganic materials 0.000 claims abstract description 9
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229910052714 tellurium Inorganic materials 0.000 claims abstract description 9
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 claims abstract description 9
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910001882 dioxygen Inorganic materials 0.000 claims abstract description 5
- 239000002638 heterogeneous catalyst Substances 0.000 claims abstract description 5
- 239000000758 substrate Substances 0.000 claims description 24
- 238000002360 preparation method Methods 0.000 claims description 15
- WBJZTOZJJYAKHQ-UHFFFAOYSA-K iron(3+) phosphate Chemical compound [Fe+3].[O-]P([O-])([O-])=O WBJZTOZJJYAKHQ-UHFFFAOYSA-K 0.000 claims description 14
- 229910000398 iron phosphate Inorganic materials 0.000 claims description 11
- 229910052751 metal Inorganic materials 0.000 claims description 11
- 239000002184 metal Substances 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 11
- BHIWKHZACMWKOJ-UHFFFAOYSA-N methyl isobutyrate Chemical group COC(=O)C(C)C BHIWKHZACMWKOJ-UHFFFAOYSA-N 0.000 claims description 10
- 239000002253 acid Substances 0.000 claims description 9
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 7
- 230000003647 oxidation Effects 0.000 claims description 7
- 238000007254 oxidation reaction Methods 0.000 claims description 7
- 238000001354 calcination Methods 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
- WDAXFOBOLVPGLV-UHFFFAOYSA-N isobutyric acid ethyl ester Natural products CCOC(=O)C(C)C WDAXFOBOLVPGLV-UHFFFAOYSA-N 0.000 claims description 5
- 239000001301 oxygen Substances 0.000 claims description 5
- 229910052760 oxygen Inorganic materials 0.000 claims description 5
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 5
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 4
- 239000011630 iodine Substances 0.000 claims description 4
- 229910052740 iodine Inorganic materials 0.000 claims description 4
- 238000005839 oxidative dehydrogenation reaction Methods 0.000 claims description 3
- 150000007513 acids Chemical class 0.000 claims description 2
- 239000003513 alkali Substances 0.000 claims description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 2
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 2
- 230000015572 biosynthetic process Effects 0.000 claims description 2
- 238000011161 development Methods 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 238000002474 experimental method Methods 0.000 claims description 2
- 239000011159 matrix material Substances 0.000 claims description 2
- 238000012986 modification Methods 0.000 claims description 2
- 230000004048 modification Effects 0.000 claims description 2
- 150000002763 monocarboxylic acids Chemical class 0.000 claims description 2
- 239000012071 phase Substances 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 2
- 229910052721 tungsten Inorganic materials 0.000 claims description 2
- 239000010937 tungsten Substances 0.000 claims description 2
- 229910052720 vanadium Inorganic materials 0.000 claims description 2
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 claims description 2
- 239000012808 vapor phase Substances 0.000 claims description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 12
- 229910052742 iron Inorganic materials 0.000 abstract description 6
- 229910019142 PO4 Inorganic materials 0.000 abstract description 3
- 235000021317 phosphate Nutrition 0.000 abstract description 3
- 150000003013 phosphoric acid derivatives Chemical class 0.000 abstract description 3
- 125000005907 alkyl ester group Chemical group 0.000 abstract 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 10
- 239000000243 solution Substances 0.000 description 7
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- 235000012239 silicon dioxide Nutrition 0.000 description 5
- 238000007613 slurry method Methods 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 238000013459 approach Methods 0.000 description 3
- 229910052681 coesite Inorganic materials 0.000 description 3
- 229910052906 cristobalite Inorganic materials 0.000 description 3
- 239000012153 distilled water Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- QZRHHEURPZONJU-UHFFFAOYSA-N iron(2+) dinitrate nonahydrate Chemical compound O.O.O.O.O.O.O.O.O.[Fe+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O QZRHHEURPZONJU-UHFFFAOYSA-N 0.000 description 3
- 238000001556 precipitation Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 229910052682 stishovite Inorganic materials 0.000 description 3
- 239000004408 titanium dioxide Substances 0.000 description 3
- 229910052905 tridymite Inorganic materials 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 229910001463 metal phosphate Inorganic materials 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- 229910005335 FePt Inorganic materials 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- AMHXQVUODFNFGR-UHFFFAOYSA-K [Ag+3].[O-]P([O-])([O-])=O Chemical class [Ag+3].[O-]P([O-])([O-])=O AMHXQVUODFNFGR-UHFFFAOYSA-K 0.000 description 1
- GGVMCOCDYREQIN-UHFFFAOYSA-K [Fe+2].P(=O)([O-])([O-])[O-].[La+3] Chemical compound [Fe+2].P(=O)([O-])([O-])[O-].[La+3] GGVMCOCDYREQIN-UHFFFAOYSA-K 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000011363 dried mixture Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000008246 gaseous mixture Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- FYDKNKUEBJQCCN-UHFFFAOYSA-N lanthanum(3+);trinitrate Chemical compound [La+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O FYDKNKUEBJQCCN-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229910001465 mixed metal phosphate Inorganic materials 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 150000003378 silver Chemical class 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- LAJZODKXOMJMPK-UHFFFAOYSA-N tellurium dioxide Chemical compound O=[Te]=O LAJZODKXOMJMPK-UHFFFAOYSA-N 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/02—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
- C07C57/03—Monocarboxylic acids
- C07C57/04—Acrylic acid; Methacrylic acid
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/14—Phosphorus; Compounds thereof
- B01J27/16—Phosphorus; Compounds thereof containing oxygen, i.e. acids, anhydrides and their derivates with N, S, B or halogens without carriers or on carriers based on C, Si, Al or Zr; also salts of Si, Al and Zr
- B01J27/18—Phosphorus; Compounds thereof containing oxygen, i.e. acids, anhydrides and their derivates with N, S, B or halogens without carriers or on carriers based on C, Si, Al or Zr; also salts of Si, Al and Zr with metals other than Al or Zr
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/14—Phosphorus; Compounds thereof
- B01J27/16—Phosphorus; Compounds thereof containing oxygen, i.e. acids, anhydrides and their derivates with N, S, B or halogens without carriers or on carriers based on C, Si, Al or Zr; also salts of Si, Al and Zr
- B01J27/18—Phosphorus; Compounds thereof containing oxygen, i.e. acids, anhydrides and their derivates with N, S, B or halogens without carriers or on carriers based on C, Si, Al or Zr; also salts of Si, Al and Zr with metals other than Al or Zr
- B01J27/1802—Salts or mixtures of anhydrides with compounds of other metals than V, Nb, Ta, Cr, Mo, W, Mn, Tc, Re, e.g. phosphates, thiophosphates
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/14—Phosphorus; Compounds thereof
- B01J27/185—Phosphorus; Compounds thereof with iron group metals or platinum group metals
- B01J27/1853—Phosphorus; Compounds thereof with iron group metals or platinum group metals with iron, cobalt or nickel
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
- C07C51/377—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Priority Applications (12)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/124,030 US4298755A (en) | 1980-02-25 | 1980-02-25 | Catalytic oxydehydrogenation process |
| SE8105937A SE435925B (sv) | 1980-02-25 | 1981-10-07 | Forfarande for katalytisk omvandling av isosmorsyra eller metylisobutyrat |
| GB08130549A GB2107305A (en) | 1980-02-25 | 1981-10-09 | Catalytic oxydehydrogenation |
| CA000387725A CA1162936A (en) | 1980-02-25 | 1981-10-09 | Oxydehydrogenation catalyst |
| ZA817089A ZA817089B (en) | 1980-02-25 | 1981-10-14 | Oxydehydrogenation catalyst |
| FR8119520A FR2514756B1 (fr) | 1980-02-25 | 1981-10-16 | Procede de conversion catalytique de l'acide butyrique ou d'un de ses equivalents fonctionnels en le derive a insaturation a,b-ethylenique correspondant par oxydeshydrogenation |
| CH6706/81A CH653005A5 (en) | 1980-02-25 | 1981-10-20 | Oxydehydrogenation catalyst, and process for the catalytic conversion of isobutyric acid or functional derivatives thereof into corresponding alpha, beta-unsaturated compounds |
| JP56166520A JPS5872537A (ja) | 1980-02-25 | 1981-10-20 | イソ酪酸またはイソ酪酸メチルを接触的に転化する方法 |
| NL8104803A NL8104803A (nl) | 1980-02-25 | 1981-10-23 | Werkwijze voor de katalytische omzetting van isoboterzuur of een functioneel equivalent tot het overeenkomstige alfa, beta- ethenisch onverzadigde derivaat. |
| BR8107073A BR8107073A (pt) | 1980-02-25 | 1981-10-30 | Processo para a conversao catalitica do acido isobutirico |
| DE3143152A DE3143152C2 (de) | 1980-02-25 | 1981-10-30 | Verfahren zur Umwandlung von Isobuttersäure oder einem Isobuttersäure-Niederalkylester in die entsprechenden α,β-äthylenisch ungesättigten Derivate durch Oxydehydrierung |
| DD81234498A DD201999A5 (de) | 1980-02-25 | 1981-10-30 | Verfahren zur katalytischen umwandlung von isobuttersaeure in das entsprechende alpha, beta-aethylenisch ungesaettigte derivat |
Applications Claiming Priority (12)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/124,030 US4298755A (en) | 1980-02-25 | 1980-02-25 | Catalytic oxydehydrogenation process |
| SE8105937A SE435925B (sv) | 1980-02-25 | 1981-10-07 | Forfarande for katalytisk omvandling av isosmorsyra eller metylisobutyrat |
| GB08130549A GB2107305A (en) | 1980-02-25 | 1981-10-09 | Catalytic oxydehydrogenation |
| CA000387725A CA1162936A (en) | 1980-02-25 | 1981-10-09 | Oxydehydrogenation catalyst |
| ZA817089A ZA817089B (en) | 1980-02-25 | 1981-10-14 | Oxydehydrogenation catalyst |
| FR8119520A FR2514756B1 (fr) | 1980-02-25 | 1981-10-16 | Procede de conversion catalytique de l'acide butyrique ou d'un de ses equivalents fonctionnels en le derive a insaturation a,b-ethylenique correspondant par oxydeshydrogenation |
| CH6706/81A CH653005A5 (en) | 1980-02-25 | 1981-10-20 | Oxydehydrogenation catalyst, and process for the catalytic conversion of isobutyric acid or functional derivatives thereof into corresponding alpha, beta-unsaturated compounds |
| JP56166520A JPS5872537A (ja) | 1980-02-25 | 1981-10-20 | イソ酪酸またはイソ酪酸メチルを接触的に転化する方法 |
| NL8104803A NL8104803A (nl) | 1980-02-25 | 1981-10-23 | Werkwijze voor de katalytische omzetting van isoboterzuur of een functioneel equivalent tot het overeenkomstige alfa, beta- ethenisch onverzadigde derivaat. |
| BR8107073A BR8107073A (pt) | 1980-02-25 | 1981-10-30 | Processo para a conversao catalitica do acido isobutirico |
| DE3143152A DE3143152C2 (de) | 1980-02-25 | 1981-10-30 | Verfahren zur Umwandlung von Isobuttersäure oder einem Isobuttersäure-Niederalkylester in die entsprechenden α,β-äthylenisch ungesättigten Derivate durch Oxydehydrierung |
| DD81234498A DD201999A5 (de) | 1980-02-25 | 1981-10-30 | Verfahren zur katalytischen umwandlung von isobuttersaeure in das entsprechende alpha, beta-aethylenisch ungesaettigte derivat |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH653005A5 true CH653005A5 (en) | 1985-12-13 |
Family
ID=27582860
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH6706/81A CH653005A5 (en) | 1980-02-25 | 1981-10-20 | Oxydehydrogenation catalyst, and process for the catalytic conversion of isobutyric acid or functional derivatives thereof into corresponding alpha, beta-unsaturated compounds |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US4298755A (is") |
| JP (1) | JPS5872537A (is") |
| BR (1) | BR8107073A (is") |
| CA (1) | CA1162936A (is") |
| CH (1) | CH653005A5 (is") |
| DD (1) | DD201999A5 (is") |
| DE (1) | DE3143152C2 (is") |
| FR (1) | FR2514756B1 (is") |
| GB (1) | GB2107305A (is") |
| NL (1) | NL8104803A (is") |
| SE (1) | SE435925B (is") |
| ZA (1) | ZA817089B (is") |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4742035A (en) * | 1980-12-31 | 1988-05-03 | The Standard Oil Co. | Mixed metal phosphorus oxide catalysts for the oxidative dehydrogenation of carboxylic acids |
| US4864057A (en) * | 1980-12-31 | 1989-09-05 | Pedersen S Erik | Dehydrogenation of carboxylic acids with mixed metal phosphorus oxide catalysts |
| AU527862B2 (en) * | 1981-01-07 | 1983-03-24 | Ashland Oil, Inc. | Oxydehydration catalyst |
| US4355176A (en) * | 1981-11-09 | 1982-10-19 | Ashland Oil, Inc. | Oxydehydrogenation process for preparing methacrylic acid and its lower alkyl esters |
| US4390725A (en) * | 1981-11-19 | 1983-06-28 | Ashland Oil, Inc. | Oxydehydrogenation process for preparing methacrylic acid and its lower alkyl esters |
| US4410728A (en) * | 1982-04-19 | 1983-10-18 | Ashland Oil, Inc. | Oxydehydrogenation process |
| US4638124A (en) * | 1984-09-21 | 1987-01-20 | Itt Corporation | Key telephone system with distributed control |
| FR2635521B1 (fr) * | 1988-08-16 | 1991-02-22 | Norsolor Sa | Procede perfectionne pour la fabrication de methacrylate de methyle a partir d'acide isobutyrique |
| US5001102A (en) * | 1989-01-11 | 1991-03-19 | Pq Corporation | Heterogeneous catalysts |
| JP2007519517A (ja) * | 2004-01-30 | 2007-07-19 | ビーエーエスエフ アクチェンゲゼルシャフト | 触媒活性組成物及びその脱水素法における使用 |
| FR2921361B1 (fr) * | 2007-09-20 | 2012-10-12 | Arkema France | Procede de fabrication d'acroleine a partir de glycerol |
| EP2179981A1 (en) | 2008-10-24 | 2010-04-28 | Arkema France | Process for manufacturing acrolein from glycerol |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3917673A (en) * | 1973-10-26 | 1975-11-04 | Eastman Kodak Co | Catalytic process for the manufacture of unsaturated acids and esters |
| US3855279A (en) * | 1973-10-26 | 1974-12-17 | Eastman Kodak Co | Catalytic process for the manufacture of unsaturated acids and esters |
| JPS5949214B2 (ja) * | 1976-11-24 | 1984-12-01 | 三菱レイヨン株式会社 | 不飽和カルボン酸またはそのエステルの製法 |
-
1980
- 1980-02-25 US US06/124,030 patent/US4298755A/en not_active Expired - Lifetime
-
1981
- 1981-10-07 SE SE8105937A patent/SE435925B/sv not_active IP Right Cessation
- 1981-10-09 CA CA000387725A patent/CA1162936A/en not_active Expired
- 1981-10-09 GB GB08130549A patent/GB2107305A/en not_active Withdrawn
- 1981-10-14 ZA ZA817089A patent/ZA817089B/xx unknown
- 1981-10-16 FR FR8119520A patent/FR2514756B1/fr not_active Expired
- 1981-10-20 JP JP56166520A patent/JPS5872537A/ja active Granted
- 1981-10-20 CH CH6706/81A patent/CH653005A5/de not_active IP Right Cessation
- 1981-10-23 NL NL8104803A patent/NL8104803A/nl not_active Application Discontinuation
- 1981-10-30 DE DE3143152A patent/DE3143152C2/de not_active Expired
- 1981-10-30 DD DD81234498A patent/DD201999A5/de not_active IP Right Cessation
- 1981-10-30 BR BR8107073A patent/BR8107073A/pt unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE3143152C2 (de) | 1985-07-25 |
| FR2514756A1 (fr) | 1983-04-22 |
| JPH0219813B2 (is") | 1990-05-07 |
| DE3143152A1 (de) | 1983-05-11 |
| SE8105937L (sv) | 1983-04-08 |
| BR8107073A (pt) | 1983-05-31 |
| GB2107305A (en) | 1983-04-27 |
| DD201999A5 (de) | 1983-08-24 |
| JPS5872537A (ja) | 1983-04-30 |
| ZA817089B (en) | 1982-09-29 |
| CA1162936A (en) | 1984-02-28 |
| US4298755A (en) | 1981-11-03 |
| SE435925B (sv) | 1984-10-29 |
| FR2514756B1 (fr) | 1986-12-26 |
| NL8104803A (nl) | 1983-05-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased | ||
| PL | Patent ceased |